Postée il y a 3 jours
La société SEBIA, société « Made in France » créée en 1967, est un acteur spécialisé dans le diagnostic in vitro et le premier fournisseur mondial d'équipements et de réactifs d'électrophorèse protéique clinique pour le dépistage et la surveillance de diverses maladies.
Entreprise à taille humaine avec environ 1200 collaborateurs à travers le monde et internationale grâce à notre présence dans plus de 120 pays dans le monde.
Dynamique à travers un très grand nombre de projets en pleine expansion se traduisant par l'ouverture de nouvelles filiales chaque année !
La mission de Sebia est de fournir des outils puissants qui traduisent ce qui se passe dans le corps d'un patient dans un langage lisible et interprétable. Nous l'appelons notre nouveau langage de vie.
Reporting to the Software Development Manager, you will BE responsible for the specification, traceability of requirements and testing of software in our product range, to meet the needs of end-users with a variety of profiles.
Tasks :
* Define detailed software functional architectures and contribute to system architecture.
* Contribute to the drafting and review of high-level requirements (User needs, System specifications).
* Write requirements and technical documentation for all software components and their interfaces, and update them with new versions and configurations.
* Standardize requirements that can BE re-used in several projects.
* Ensure traceability of requirements, interfaces and tests.
* Ensure the quality of deliverables through precise definition of technical specifications at several levels, while optimizing their number.
* Model use cases using UML or equivalent diagrams.
* Implement the principles of software operational safety and cybersecurity through standardized requirements approved by the RA/QA department.
* Assist in drafting test plans and evaluate test results of developed software components.
* Control and maintain software risk analysis.
* Implement continuous software integration processes.
* Contribute to the implementation of work methods and tools enabling requirements Management and Full tracability with tests.
Technical Skills :
* 5 to 10 years' experience in medical software development in a small development team (ideally 5 to 20 people).
* Knowledge of the following technologies : UML, Azure Dev. Ops or other requirements management software (e.g.JAMA)
* Expert in IEC 62 304
* Knowledge of ISO 13 485, FDA 21 CFR 820
* Fluency in written and spoken English.
Soft Skills :
* Rigor and organization.
* Creativity, sense of innovation.
* Adaptability and flexibility.
* Team Spirit.
Technical Skills :
* 5 to 10 years' experience in medical software development in a small development team (ideally 5 to 20 people).
* Knowledge of the following technologies : UML, Azure Dev. Ops or other requirements management software (e.g.JAMA)
* Expert in IEC 62 304
* Knowledge of ISO 13 485, FDA 21 CFR 820
* Fluency in written and spoken English.
Soft Skills :
* Rigor and organization.
* Creativity, sense of innovation.
* Adaptability and flexibility.
* Team Spirit.